GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glpS in Paraburkholderia bryophila 376MFSha3.1

Align GlpS, component of Glycerol uptake porter, GlpSTPQV (characterized)
to candidate H281DRAFT_01451 H281DRAFT_01451 carbohydrate ABC transporter ATP-binding protein, CUT1 family

Query= TCDB::G3LHY8
         (358 letters)



>FitnessBrowser__Burk376:H281DRAFT_01451
          Length = 415

 Score =  196 bits (499), Expect = 7e-55
 Identities = 123/360 (34%), Positives = 182/360 (50%), Gaps = 20/360 (5%)

Query: 4   LRNAAKMVGADYHIYPTDLVLERGTLNVLLGPTLAGKTSLMRLMAGLDRPTGGSIHFDGT 63
           +RN    +G +  I   DL ++ G   VLLGP+  GK++L+  +AGL   T GSI   G 
Sbjct: 50  VRNLTIRLGGNTVIENLDLDVQPGEFVVLLGPSGCGKSTLLHSIAGLIDVTDGSIEIAGE 109

Query: 64  DVTGMPVQKRNVAMVYQQFINYPALTVYNNIASPMRISGKDAATIDREVRKAAELLKLTP 123
           D+T    + R +A+V+Q +  YP ++V  N++  +RI+G   A I R V +AAE+L+L P
Sbjct: 110 DMTWADPKDRRIALVFQSYALYPTMSVERNLSFALRINGTPKAEIARRVARAAEMLQLGP 169

Query: 124 YLDRTPLNLSGGQQQRTALARALVKNASLVLMDEPLANLDYKLREELREELPKIFAQSGA 183
            L R P  LSGGQ+QR A+ RA+V+ A + L DEPL+NLD KLR ELR EL ++  + GA
Sbjct: 170 LLKRKPAQLSGGQRQRVAIGRAIVREADVFLFDEPLSNLDAKLRTELRRELKQLHQRLGA 229

Query: 184 IFVYATTEPSEALLLGGNTATLNQGRVTQFGPTIEVYRRPVNLATAGIFADPPLNTLDVT 243
             +Y T +  EA++L    A +  G + QFG   EVY RP NL  A     P +N ++ T
Sbjct: 230 TMIYVTHDQVEAMMLATRMAVMRGGAIQQFGTPAEVYARPANLFVATFLGTPAMNLVNGT 289

Query: 244 ------------------KSGNVFTRPSGVTIPVPSHLAVVPDGPVTIAFHPHHLGLAPQ 285
                              S   F   SG + P     +  P  P  +      + + P 
Sbjct: 290 LEQRDGALHFCTEQWRLDVSNYAFVDRSGESQPQSQPQS--PPRPCVLGVRAEDVRIGPT 347

Query: 286 TGDAARLQARTLVSEITGSESFVHLEYDGVRWVMLAHGIHDIDPDMEVEAFLDTRHLMAF 345
            G+ A   A+  + E  G+   V L+Y GV+   +      + P   +   LD+ H+  F
Sbjct: 348 QGEGAGEHAKISLVEPMGNHRVVWLDYHGVQIASIDQSKTPVMPGDTLAFSLDSTHVSLF 407


Lambda     K      H
   0.319    0.136    0.392 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 351
Number of extensions: 13
Number of successful extensions: 2
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 358
Length of database: 415
Length adjustment: 30
Effective length of query: 328
Effective length of database: 385
Effective search space:   126280
Effective search space used:   126280
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory